Skip to content

Vascular Cardiotoxicity of Ponatinib

Vascular Cardiotoxicity of Ponatinib

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03930394
Enrollment
32
Registered
2019-04-29
Start date
2019-05-15
Completion date
2022-05-01
Last updated
2019-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiotoxicity

Brief summary

Pre-clinical studies suggest that the third generation tyrosine kinase inhibitor ponatinib can result in microvascular angiopathy and acceleration of atherosclerosis. This study is intended to examine for myocardial microvascular angiopathy and changes in carotid plaque in patients receiving ponatinib as part of their clinical care.

Detailed description

In this study, we will perform serial echocardiography for ventricular function, myocardial contrast echocardiography for microvascular perfusion assessment, blood analysis for myocardial injury, and carotid US for plaque or IMT progression in subjects receiving ponatinib. This series of tests is intended to provide information on the presence of clinically-evident or subclinical microvascular angiopathy and plaque acceleration.

Interventions

DIAGNOSTIC_TESTContrast ultrasound perfusion imaging

Contrast ultrasound perfusion imaging for microvascular perfusion, and carotid ultrasound data on intima-media thickness (or plaque size) will be serially assessed in subjects started on ponatinib.

Sponsors

Oregon Health and Science University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years

Inclusion criteria

* Diagnosis of CML or ALL * Prescribed ponatinib

Exclusion criteria

* pregnancy or lactation * major medical illness involving the heart or vasculature (CAD, PAD, DCM). * hemodynamically unstable * allergy to ultrasound contrast agents.

Design outcomes

Primary

MeasureTime frameDescription
Presence versus absence of any myocardial perfusion defect assessed by visual analysis for any abnormalities of microvascular flux rate (beta function) or microvascular blood volume during an infusion of ultrasound microbubble contrast agents.6 monthsContrast ultrasound perfusion imaging will be performed using power-modulation imaging and infusion of an ultrasound contrast agent. Destruction replenishment kinetics will be assessed visually by examination of delayed replenishment of signal intensity (\>5 seconds) after a high-mechanical index burst sequence, or abnormalities in plateau intensity reflecting regional abnormalities in myocardial microvascular blood volume.
Carotid plaque size6 monthsChanges in IMT or plaque size

Countries

United States

Contacts

Primary ContactMelinda Wu, MD
wume@ohsu.edu503 494-4772

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026